List of variants in gene XIAP reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001167.4(XIAP):c.1096A>G (p.Ile366Val)	rs766720607	0.00008
NM_001167.4(XIAP):c.308C>T (p.Thr103Met)	rs749157868	0.00001
NM_001167.4(XIAP):c.819G>A (p.Gly273=)	rs2148090248
NM_001167.4(XIAP):c.878-5C>T	rs367801081

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